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SHIFT | HOURS: overnight shift | 12 hours shift | 2-2-3 schedule. Directs maintenance crews in the installation, repair and preventive maintenance of equipment used throughout the plant, facilities, utilities and powerhouse equipment.. Advanced technical skills in ammonia refrigeration, high pressure boiler, compressed air, mechanical and electrical fields (e.g. PLCs, instrumentation, mechanical engineering, etc.). Thorough knowledge of maintenance systems, work order processes, preventive/predictive maintenance, TPM, inventory and scheduling software, preferred.. Strong leadership skills (conflict resolution, facilitation, change management skills, decision making, empowerment and delegation), preferred.
· Ensure adherence to Lean Methodology, including Kaizen, 5S, Standard Work, Daily Management, Layered Audit Process and Business Plan development to eliminate waste. Has knowledge in the areas of: 5S, SMED, TPM, VSM, PDCA or equivalent, A3 Problem Solving. Partner with Operating Unit Continuous Improvement Manager to ensure process improvement projects are completed timely and on budget. Experience with Six Sigma, Lean Processes, Automation and SAP strongly preferred. The Pactiv Evergreen Raleigh Carton Converting Facility is located in Raleigh, North Carolina, which is also home to North Carolina State University and the state's capitol.
Lead Continuous Improvement – Utilize Lean principles, SPC, and DOE methodologies to analyze data, drive corrective actions, and optimize manufacturing processes.. Drive Supplier Quality Management – Work with vendors to establish and maintain quality expectations, ensuring reliable and consistent product performance.. Develop Quality Training Programs – Train internal teams on quality control processes, SPC, and corrective action strategies , fostering a culture of continuous improvement.. Experience – 3-5+ years of experience in quality control, process auditing, lean manufacturing, or engineering within a manufacturing environment.. Certifications (Preferred) – Six Sigma Green or Black Belt certification.
Our Company: C/A Design is part of the Heico Companies, and in the aggregate, Heico’s businesses generate more than $3.2 billion in revenues.. Deliver industry-leading quality, and on-time delivery while providing an exceptional customer experience.. Additionally, the Senior Manufacturing Engineer maximizes product efficiency by analyzing layout of equipment, workflow, assembly methods, and work force utilization.. Develops, evaluates, and improves manufacturing methods, utilizing knowledge of product design, materials and parts, fabrication processes, tooling and production equipment capabilities, assembly methods, and quality control standards.. Leads plant management and employees in conceptualizing, planning and implementing, and sustaining continuous improvements by utilizing Lean Manufacturing tools.
The MSI Express Leadership Rotational Program is a two-year developmental program designed to provide hands-on experience in 3-4 different departments within MSI Express.. This program is designed to provide a well-rounded understanding of food manufacturing, supply chain logistics, financial planning, customer engagement, and human capital management.. Supply Chain – Understand logistics, inventory management, scheduling, and demand planning to optimize product flow and minimize disruptions.. Quality Assurance – Learn about compliance with food safety standards and regulatory guidelines, gaining expertise in FDA, NSF, and SQF requirements and standards.. ✅ No prior work experience required, but internship or co-op experience is a plus
The Director of Operations will oversee both long-term strategic planning and daily operations related to the manufacturing of a segment of the CCM business.. to include PD projects, MDI, 5S, TPM, kaizen and best practice sharing amongst plants.. Collaborate with sales, demand/supply planning, engineering, safety, quality and other cross functional teams to proactively develop companywide manufacturing product and service solutions.. Champion annual efforts to build the Polyurethane and Rubber operating and capital budgets.. Individual will operate primarily in an office setting, with an option to perform job duties in a fully remote capacity, with frequent travel
A large medical device manufacturing client is looking for a direct hire Senior Automation Engineer to join their Mebane, NC site.. This person will report to the Facilities & Maintenance Manager and support the key business objectives through production support and assigned plant specific projects, the associate drives activities to deliver upon these objectives.. Process control, batch processing, SCADA and MES. Technical Writing skills as applied to manufacturing documentation and process development. Advanced proficiency in PLC diagnostics and programming, MES experience a plus.
A world leader in the field of in vitro diagnostics for more than 60 years, bioMerieux provides diagnostic solutions which determine the source of disease and contamination to improve patient health and ensure consumer safety.. High School Diploma/GED with 4+ years of experience in electro-mechanical maintenance, troubleshooting and repairing of electro-mechanical systems.. Associate's Degree and 2+ years of experience in electro-mechanical maintenance, troubleshooting and repairing of electro-mechanical systems.. Strong attention to detail and GMP experience (including knowledge of change control, validation, and commissioning processes) desired.. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMerieux's or its affiliates' application process by contacting us via telephone at , by email at , or by dialing 711 for access to Telecommunications Relay Services (TRS).
Adherence to FDA Regulations, GMP, ISO, HSE (OSHA), Department Procedures, and Manufacturing Directions.. Required: High School Diploma/GED with 7+ years of maintenance experience on electro-mechanical systems.. Experience in a manufacturing environment working on production equipment is highly desired Ability to read ladder logic, troubleshoot and repair PLC’s, electrical systems, AC/DC drive systems, and mechanical systems preferred.. Preferred: Associates degree in electronics technology or related field with 5+ years maintenance experience focused on support of production equipment.. Knowledge of change control, validation, and commissioning processes.
Provides technical safety and health support and information to HAI safety director.. Assists with implementation and maintenance of controls to minimize safety and occupational health hazards.. An AA degree in mechanical, electrical, or industrial maintenance/engineering a plus.. IPG Laser Systems, Siemens CNC, Allen Bradley PLC, Fanuc/Kuka Robotic experience a plus.. Strong mechanical aptitude with ability to use shop hand and power tools.
Piper Companies is actively seeking a Validation and Technical Support Engineer to join a global pharmaceutical organization producing innovative, injectable diabetes and obesity treatment.. Take ownership of Change Requests (CRs) related to project validation responsibilities.. Experience with IT systems such as PAS-X, SAP, and Aveva PI, and computerized equipment such as autoclaves, packaging, assembly, filling, cart washers, utensil washers, CIP/SIP, and formulation.. Qualifications of the Validation and Technical Support Engineer: BA/BS degree in Engineering, Computer Science, or applicable technical degree or proven equivalent relevant work experience.. Experience in pharmaceutical manufacturing preferred.
With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year.. Direct knowledge of design and troubleshooting with GMP Biopharmaceutical Production facility equipment/ systems needed to support these processes such as autoclaves, clean in place (CIP) systems, washers, clean steam, water for injection, etc.. Ability to analyze problems, develop and propose engineering solutions in a scientific manner using data-driven techniques and analyses (e.g., Data Analytics, Root Cause Analysis (RCA), Statistical Process Control (SPC), Six Sigma, Predictive Maintenance, etc.. and familiarity with GMP quality systems/processes such as change control, non-conformances, corrective and preventative actions, and qualifications/validation. Understanding of capital projects in a GMP Biopharmaceutical Production facility including procurement, construction, startup, and validation
Strong attention to detail which translates in SOP authoring, developing training tools, and improving user interface in MES or HMIs. Participates and/or lead cross functional teams in the development and implementation of strategies associated with the area for the following initiatives: Continuous Improvement, Root Cause Analysis (RCA), Failure Modes Effect Analysis (FMEA), Operational Standards for Supply Chain Excellence (OSSCE).. Work with EWM, IDS and Master Data Team to support launch and ticket builds and process order releases.. Experienced as a technician/operator in a pharmaceutical manufacturing environment.. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities).
With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year.. When completed, the Amgen FleX Batch facility will combine the latest in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations.. The FleX Batch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen‘s plan to be a carbon-neutral company by 2027.. 3+ years of experience with regulated environments (i.e. cGMP, OSHA, EPA). Experience working with ATO GMP F&E clients and systems (Bulk Manufacturing, Filling and Packaging, Supply Chain, Quality Labs, Small Molecule Manufacturing)
Our Avionics team advances flight deck solutions, airborne communications, vision systems, sensors and fire protection for commercial and military customers around the world.. Collins Aerospace, a RTX company, is a leader in technologically advanced and intelligent solutions for the global aerospace and defense industry.. Collins Aerospace has the capabilities, comprehensive portfolio and expertise to solve customers’ toughest challenges and to meet the demands of a rapidly evolving global market.. Get onboard the Collins Aerospace Operations team and play a part in managing our innovative products from inception to delivery.. The Operations team continues to grow and aims to strengthen the connection of Manufacturing Operations, Supply Chain and Environment, Health & Safety (EH&S) across Collins Aerospace.
We’re building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.. Lead risk assessments and author technical reports for enrollment of new raw materials and components.. Hands-on experience with the management of Change Controls, Deviations and CAPA is required.. Minimum of 7 years of pharmaceutical or biopharmaceutical industry experience, with a minimum of 5 years in Quality Control, Quality Systems or Quality Assurance.. Resilience offers employees a robust total rewards program including equity, an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, flexible time off, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs.
Piper Companies is searching for a Utilities Maintenance Technician for a full time position at a pharmaceutical organization in the Greater Raleigh, NC region.. The Utilities Maintenance Technician will be responsible for the continuous improvement and preventative maintenance of utility systems throughout the pharmaceutical facility.. There is day-shift and night-shift available depending on preference.. Knowledgeable with most of the following preferred:Compressed air, HVAC, refrigeration systems, high pressure/low pressure steam, clean/purified steam, WFI systems, chill water systems, instrumentation & electrical systems. Keywords: technician, maintenance, maintenance technician, pharma, pharmaceutical, pharmaceutical maintenance jobs, utilities, utilities maintenance, industrial, industrial manufacturing, regulatory, HVAC, WFI, facilities, facilities technician, faculties jobs
Position Summary: This position reports to the Customer Service Manager and is responsible for providing Professional customer service and ensuring the organization understands and adheres to its customer’s requirements.. This position will be the key liaison between the company and its customers and will ensure the order process is executed accurately, including receiving the order, order entry, establishing available-to-promise via current inventory or production, order shipment and tracking, order delivery, and customer invoicing; all while keeping internal and external parties apprised of the order status.. 4) Ensure Order shipment and tracking, order delivery, and customer invoicing within 24 hours of shipment. Maintain accurate estimated Ship Dates for orders by communicating and coordinating with the Site Production and Logistics Coordinator as well as Production Distribution Planner to define date based on input supply and the production schedule. Prior agriculture knowledge and International shipping experience
Mfg./Pkg. Operator is to perform all required Batch manufacturing, packing, equipment cleaning, area cleaning, in- process testing & sampling for Manufacturing and Packaging batches.. Perform verifications using special instruments (Caliper, Balance, etc.). Assist the Batch manufacturing, Packing & Cleaning of the equipment machinery and area.. Complete all applicable training forms in a timely manner and forward to document control for archival.. Must be a Team player able to effectively communicate with QA Supervisor, IPQA, Quality Control, Production, Warehouse, Engineering and Supply Chain to meet finished product release goals
TRC is looking for a Packaging Engineer for a client located in Graham, NC!. Support sustainability initiatives by identifying eco-friendly packaging alternatives and improving recyclability of current packaging materials.. Bachelors degree in Packaging Engineering, Mechanical Engineering, Materials Science, or a related field.. Experience with food-grade packaging and knowledge of FDA, USDA, and other regulatory requirements is a plus.. Proficiency in CAD software (AutoCAD, SolidWorks, or similar) for designing packaging components.